Senior Medical Research Associate (EMT)

ICON plcLenexa, KS
4dOnsite

About The Position

Senior Medical Research Associate (EMT) - Lenexa, KS (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Senior Medical Research Associate (EMT Certification Required) Location: Lenexa, KS Schedule: Morning and Overnight Shifts Available Employment Type: Part- Time Overview We are seeking a highly skilled Senior Medical Research Associate with valid EMT certification to support both our clinical research operations and onsite clinic. This role blends hands‑on patient care with research responsibilities and is ideal for someone who thrives in a fast‑paced environment, is confident in emergency response, and can ensure high‑quality and compliant study execution.

Requirements

  • Active EMT certification required (EMT‑Basic, Advanced EMT, or EMT‑Paramedic depending on state requirements).
  • Experience in emergency medical care, urgent care, or other fast‑paced clinical settings.
  • Strong understanding of clinical procedures, patient care standards, and documentation practices.
  • Excellent judgment in emergency situations and the ability to maintain composure under pressure.
  • Strong organizational, multitasking, and time‑management skills.
  • Excellent communication and interpersonal skills with the ability to work effectively across clinical and research teams.
  • Ability to work assigned morning or overnight shifts as needed.

Nice To Haves

  • Prior clinical research experience preferred but not required for candidates with strong clinical and EMT backgrounds.

Responsibilities

  • Provide direct patient care within the onsite clinic, including patient assessment, vital signs, triage, and urgent clinical support.
  • Perform EMT‑level procedures within certification scope, including blood draws, specimen collection, wound care, and stabilization during urgent or unexpected clinical situations.
  • Support participant safety during research procedures and respond promptly to any medical concerns or adverse events.
  • Ensure clinical equipment and supplies are properly maintained, stocked, and ready for use.
  • Assist in planning, coordinating, and monitoring clinical research activities to ensure compliance with study protocols and regulatory requirements.
  • Support study procedures including sample handling, documentation, subject visit coordination, and protocol-driven tasks.
  • Conduct site‑level training, reinforce protocol adherence, and provide ongoing operational support to investigators and staff.
  • Track study progress, maintain accurate records, and ensure all clinical and research documentation meets quality standards.
  • Participate in the review and development of study materials such as source documents, manuals, logs, and operational tools.
  • Mentor junior Research Associates and contribute to a collaborative and high‑performance team culture.

Benefits

  • In addition to your competitive salary, ICON offers a range of additional benefits.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
  • Our benefits examples include:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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